 | One-Click MDS Generation to Simplify the Process and Minimize Errors |
 | Accurate MDS creation through integration with internal BOM systems. |
Significantly reduces MDS creation time.
| Automatic tracking of MDS submission status. |
| Automated requests for MDS from suppliers. |
Efficient MDS management reduces project delays.
| Automatic analysis of regulatory substances in products. |
| Simultaneous identification of non-compliant components and suppliers. |
Proactively prevents potential regulatory violations.
Manual MDS creation is time-consuming and prone to duplicate entries or errors.
Automation significantly reduces MDS creation time and enhances overall task efficiency.
It minimizes errors, improves data accuracy, and ensures higher-quality MDS results.
Manually identifying regulatory substances is impractical and time-consuming.
The automated solution enables fast and accurate analysis of product substances. It simplifies compliance by identifying non-compliant components in one step, ensuring adherence to global regulations.
Frequent MDS rejections increase costs, delay timelines, and harm customer relationships.
Our solution includes enhanced MDS validation tools to identify issues early, significantly reducing rejection rates.
This ensures high-quality submissions and builds stronger customer trust.
